Product NDC: | 61314-303 |
Proprietary Name: | Atropine Sulfate |
Non Proprietary Name: | atropine sulfate |
Active Ingredient(s): | 1 mg/mL & nbsp; atropine sulfate |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61314-303 |
Labeler Name: | FALCON LABORATORY LTD |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20000630 |
Package NDC: | 61314-303-01 |
Package Description: | 5 mL in 1 BOTTLE, PLASTIC (61314-303-01) |
NDC Code | 61314-303-01 |
Proprietary Name | Atropine Sulfate |
Package Description | 5 mL in 1 BOTTLE, PLASTIC (61314-303-01) |
Product NDC | 61314-303 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | atropine sulfate |
Dosage Form Name | SOLUTION |
Route Name | OPHTHALMIC |
Start Marketing Date | 20000630 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | FALCON LABORATORY LTD |
Substance Name | ATROPINE SULFATE |
Strength Number | 1 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |